Suppr超能文献

编码人白细胞唾液酸蛋白的cDNA的特性分析及白细胞唾液酸蛋白基因在16号染色体上的定位

Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16.

作者信息

Pallant A, Eskenazi A, Mattei M G, Fournier R E, Carlsson S R, Fukuda M, Frelinger J G

机构信息

Cancer Center Immunology Unit, University of Rochester Medical Center, NY 14642.

出版信息

Proc Natl Acad Sci U S A. 1989 Feb;86(4):1328-32. doi: 10.1073/pnas.86.4.1328.

Abstract

We describe the isolation and characterization of cDNA clones encoding human leukosialin, a major sialoglycoprotein of human leukocytes. Leukosialin is very closely related or identical to the sialophorin molecule, which is involved in T-cell proliferation and whose expression is altered in Wiskott-Aldrich syndrome (WAS), an X chromosome-linked immunodeficiency disease. Using a rabbit anti-serum to leukosialin, a cDNA clone was isolated from a lambda gt11 cDNA library constructed from human peripheral blood cells. This lambda gt11 clone was used to isolate longer cDNA clones that correspond to the entire coding sequence of leukosialin. DNA sequence analysis reveals three domains in the predicted mature protein. The extracellular domain is enriched for Ser, Thr, and Pro and contains four contiguous 18-amino acid repeats. The transmembrane and intracellular domains of the human leukosialin molecule are highly homologous to the rat W3/13 molecule. RNA gel blot analysis reveals two polyadenylylated species of 2.3 and 8 kilobases. Southern blot analysis suggests that human leukosialin is a single-copy gene. Analysis of monochromosomal cell hybrids indicates that the leukosialin gene is not X chromosome linked and in situ hybridization shows leukosialin is located on chromosome 16. These findings demonstrate that the primary mutation in WAS is not a defect in the structural gene for leukosialin.

摘要

我们描述了编码人白细胞涎酸蛋白(一种人白细胞的主要唾液糖蛋白)的cDNA克隆的分离和特性。白细胞涎酸蛋白与唾液酸ophorin分子密切相关或相同,后者参与T细胞增殖,其表达在威斯科特-奥尔德里奇综合征(WAS,一种X染色体连锁免疫缺陷疾病)中发生改变。使用抗白细胞涎酸蛋白的兔抗血清,从用人外周血细胞构建的λgt11 cDNA文库中分离出一个cDNA克隆。这个λgt11克隆被用于分离对应于白细胞涎酸蛋白整个编码序列的更长的cDNA克隆。DNA序列分析揭示了预测的成熟蛋白中的三个结构域。细胞外结构域富含丝氨酸、苏氨酸和脯氨酸,并包含四个连续重复的18个氨基酸序列。人白细胞涎酸蛋白分子的跨膜和细胞内结构域与大鼠W3/13分子高度同源。RNA凝胶印迹分析揭示了2.3和8千碱基的两种多聚腺苷酸化物种。Southern印迹分析表明人白细胞涎酸蛋白是一个单拷贝基因。对单染色体细胞杂种的分析表明白细胞涎酸蛋白基因不是X染色体连锁的,原位杂交显示白细胞涎酸蛋白位于16号染色体上。这些发现表明WAS中的原发性突变不是白细胞涎酸蛋白结构基因的缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e857/286683/ea1ca605c690/pnas00244-0235-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验